Variant (rsID / SNP)

rs28439342

rs28439342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WIPF3. Location: chromosome 7, position 29,923,572. The table records no clinical significance for this variant.

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Reference-table entries

WIPF3Not classified

Variant type: synonymous_variant
Chromosome / position: 7:29923572
HGVS: NM_001080529.3,c.462T>C,p.Asn154Asn
Allele change: Synonymous_N154N

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.